Malathion biodegradation and biotransformation in water and sediment systems: bacterial pathways, environmental drivers, ecological impacts, and bioremediation strategies

Malathion is one of the most widely used organophosphate insecticides, and its environmental fate is strongly influenced by microbial transformation in the water column and sediments. This review synthesizes current knowledge of the enzymatic and metabolic pathways that govern the persistence of malathion in aquatic, sedimentary, and wastewater systems. Members of the genera Pseudomonas, Bacillus, Acinetobacter, Rhodococcus, Micrococcus, and several other commonly studied taxa produce enzymes such as carboxylesterases and hydrolases that cleave the carboxyl ester linkage. The major metabolites formed are malathion monocarboxylic acid (MMC) and malathion dicarboxylic acid (MDC), which are generally far less toxic than the parent compound and, under favorable conditions, can be further mineralized to carbon dioxide and inorganic phosphate. A parallel transformation route, oxidative desulfuration, can generate malaoxon, a metabolite substantially more toxic and persistent than malathion and therefore important to consider in environmental risk assessment. Degradation rates are typically highest at 25-35 °C and neutral to slightly alkaline pH conditions that favor hydrolytic activity. Redox conditions further influence pathway predominance: oxic environments generally favor hydrolysis and oxidative transformation, whereas anoxic environments may slow overall degradation and promote alternative reductive processes. Nutrient availability can stimulate microbial growth and enzyme expression, accelerating degradation in eutrophic waters and organic-rich sediments, whereas in oligotrophic systems, transformation is often slower. Consequently, microbial activity can reduce malathion's environmental half-life from weeks to days in some systems, although the transient formation of toxic intermediates necessitates monitoring beyond the parent compound. Improved understanding of the microbial taxa, enzymatic machinery, and environmental drivers involved provides a stronger mechanistic framework for predicting malathion fate, refining ecological risk assessments, and informing targeted bioremediation strategies in contaminated ecosystems.

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Publication Details

Journal
World Journal of Microbiology and Biotechnology
Published
2026-09-06
DOI
https://doi.org/10.1007/s11274-026-05239-8
Primary Topic
Pesticide and Herbicide Environmental Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Malathion biodegradation and biotransformation in water and sediment systems: bacterial pathways, environmental drivers, ecological impacts, and bioremediation strategies

Avishek Dutta, Srimanti Duttagupta, Gayatri Basapuram
World Journal of Microbiology and Biotechnology
Pesticide and Herbicide Environmental Studies
article

Malathion biodegradation and biotransformation in water and sediment systems: bacterial pathways, environmental drivers, ecological impacts, and bioremediation strategies

Avishek Dutta, Srimanti Duttagupta, Gayatri Basapuram
article en

Abstract

Malathion is one of the most widely used organophosphate insecticides, and its environmental fate is strongly influenced by microbial transformation in the water column and sediments. This review synthesizes current knowledge of the enzymatic and metabolic pathways that govern the persistence of malathion in aquatic, sedimentary, and wastewater systems. Members of the genera Pseudomonas, Bacillus, Acinetobacter, Rhodococcus, Micrococcus, and several other commonly studied taxa produce enzymes such as carboxylesterases and hydrolases that cleave the carboxyl ester linkage. The major metabolites formed are malathion monocarboxylic acid (MMC) and malathion dicarboxylic acid (MDC), which are generally far less toxic than the parent compound and, under favorable conditions, can be further mineralized to carbon dioxide and inorganic phosphate. A parallel transformation route, oxidative desulfuration, can generate malaoxon, a metabolite substantially more toxic and persistent than malathion and therefore important to consider in environmental risk assessment. Degradation rates are typically highest at 25-35 °C and neutral to slightly alkaline pH conditions that favor hydrolytic activity. Redox conditions further influence pathway predominance: oxic environments generally favor hydrolysis and oxidative transformation, whereas anoxic environments may slow overall degradation and promote alternative reductive processes. Nutrient availability can stimulate microbial growth and enzyme expression, accelerating degradation in eutrophic waters and organic-rich sediments, whereas in oligotrophic systems, transformation is often slower. Consequently, microbial activity can reduce malathion's environmental half-life from weeks to days in some systems, although the transient formation of toxic intermediates necessitates monitoring beyond the parent compound. Improved understanding of the microbial taxa, enzymatic machinery, and environmental drivers involved provides a stronger mechanistic framework for predicting malathion fate, refining ecological risk assessments, and informing targeted bioremediation strategies in contaminated ecosystems.

World Journal of Microbiology and BiotechnologyVol. 42(9)
University of Georgia (US), Savannah River National Laboratory (US)
U.S. Department of Energy
Clean water and sanitation
Openalex Percentile: Top 21%
Pesticide and Herbicide Environmental Studies
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